A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5849966



Internal ID22624901
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:94049318..94056394hg38UCSC Ensembl
chr9:96811600..96818676hg19UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg387077
hg197077
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17514826, nssv17514825
Samples
Known GenesPTPDC1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5849966
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer